Medical Device Recalls
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1 result found
510(K) Number: K181661 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Bio-Rad, REF: 12005660, QXDx BCR-ABL %IS Kit | 2 | 03/22/2024 | Bio-Rad Laboratories |
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